BeNa Culture Collection
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| Growth conditions | 35 ℃ |
| Subculture procedure | ① Remove the cryovial from liquid nitrogen or -80 ℃ refrigerator and place it in PE gloves. Quickly immerse it in a 37 ℃ water bath, shake the cryovial to accelerate dissolution, and dissolve it completely within 1 minute; ② Add the suspension to 6-7 mL of complete culture medium and incubate in an incubator. ③ Pay attention to changes in the pH value of the culture medium and cell density. When the cell density reaches greater than 2 × 106 cells/mL, repeat the passaging operation or cryopreservation. |
| Storage conditions | Liquid nitrogen |
| Sharing mode | Public welfare sharing |
Quantitative strains of bacillus cereus(Quantitative strains of bacillus cereus)
BNCC399551
Quantitative strains of Clostridium perfringens(Quantitative strains of Clostridium perfringens)
BNCC399657
KG-1a(KG-1a)
BNCC100983
SNU-5(SNU-5)
BNCC344674
Biochemical Identification Kit for Plesiomonas shigelloides(Biochemical Identification Kit for Plesiomonas shigelloides)
BNCC390163
Biochemical Identification Kit for Alcaligenes faecalis(Biochemical Identification Kit for Alcaligenes faecalis)
BNCC390167
Sphingomonas sp. DNA standard
BNCC398140
Acholeplasma laidlawii DNA standard
BNCC397767
Human gammaherpesvirus 4 nucleic acid reference (Heat inactivated) (Strongly positive)
BNCC397551
Lachnoclostridium massiliosenegalense DNA lab quality control
BNCC397446
Trichomonas vaginalis DNA standard
BNCC397436
Trichomonas vaginalis DNA standard
BNCC397435
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